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A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst

Diamines are important industrial chemicals. In this paper we outline the feasibility of lignocellulose as a source of diol‐containing molecules. We also illustrate the possibility of turning these diols into their diamines in good to excellent yields. Central to these transformations is the use of...

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Autores principales: Wu, Xianyuan, De bruyn, Mario, Barta, Katalin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826469/
https://www.ncbi.nlm.nih.gov/pubmed/36632530
http://dx.doi.org/10.1002/cite.202200091
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author Wu, Xianyuan
De bruyn, Mario
Barta, Katalin
author_facet Wu, Xianyuan
De bruyn, Mario
Barta, Katalin
author_sort Wu, Xianyuan
collection PubMed
description Diamines are important industrial chemicals. In this paper we outline the feasibility of lignocellulose as a source of diol‐containing molecules. We also illustrate the possibility of turning these diols into their diamines in good to excellent yields. Central to these transformations is the use of commercially available Raney Ni. For diol formation, the Raney Ni engages in hydrogenation and often also demethoxylation, that way funneling multiple components to one single molecule. For diamine formation, Raney Ni catalyzes hydrogen‐borrowing mediated diamination in the presence of NH(3).
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spelling pubmed-98264692023-01-09 A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst Wu, Xianyuan De bruyn, Mario Barta, Katalin Chem Ing Tech Research Articles Diamines are important industrial chemicals. In this paper we outline the feasibility of lignocellulose as a source of diol‐containing molecules. We also illustrate the possibility of turning these diols into their diamines in good to excellent yields. Central to these transformations is the use of commercially available Raney Ni. For diol formation, the Raney Ni engages in hydrogenation and often also demethoxylation, that way funneling multiple components to one single molecule. For diamine formation, Raney Ni catalyzes hydrogen‐borrowing mediated diamination in the presence of NH(3). John Wiley and Sons Inc. 2022-09-19 2022-11 /pmc/articles/PMC9826469/ /pubmed/36632530 http://dx.doi.org/10.1002/cite.202200091 Text en © 2022 The Authors. Chemie Ingenieur Technik published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Wu, Xianyuan
De bruyn, Mario
Barta, Katalin
A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst
title A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst
title_full A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst
title_fullStr A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst
title_full_unstemmed A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst
title_short A Diamine‐Oriented Biorefinery Concept Using Ammonia and Raney Ni as a Multifaceted Catalyst
title_sort diamine‐oriented biorefinery concept using ammonia and raney ni as a multifaceted catalyst
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826469/
https://www.ncbi.nlm.nih.gov/pubmed/36632530
http://dx.doi.org/10.1002/cite.202200091
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